Canonical Allele Identifier: CA2832529142

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771981_116772006del , CM000669.2:g.116771981_116772006del	GRCh38
NC_000007.13:g.116412035_116412060del , CM000669.1:g.116412035_116412060del	GRCh37
NC_000007.12:g.116199271_116199296del	NCBI36
NG_008996.1:g.104577_104602del , LRG_662:g.104577_104602del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*625_*633+17del
ENST00000318493.11:c.3074_3082+17del
ENST00000397752.8:c.3020_3028+17del
ENST00000318493.10:c.3074_3082+17del
ENST00000397752.7:c.3020_3028+17del
ENST00000454623.1:c.283+327_283+352del	ENSP00000398140.1:n.283+327_283+352del
NM_000245.2:c.3020_3028+17del
NM_001127500.1:c.3074_3082+17del , LRG_662t1:c.3074_3082+17del
XM_006715990.2:c.1730_1738+17del
XM_006715991.2:c.1730_1738+17del
XM_011516223.1:c.3077_3085+17del
NM_000245.3:c.3020_3028+17del
NM_001127500.2:c.3074_3082+17del
NM_001324402.1:c.1730_1738+17del
XR_001744772.1:n.3151_3159+17del
NM_001127500.3:c.3074_3082+17del
NM_000245.4:c.3020_3028+17del
NM_001324402.2:c.1730_1738+17del